Evaluation and Treatment of Crown Fractures Using the Modified Baysal Dental Trauma Index

NCT07131462 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 39

Last updated 2025-08-20

No results posted yet for this study

Summary

This study will be conducted by the Department of Pediatric Dentistry, Faculty of Dentistry, İnönü University, with the aim of evaluating the treatment processes and follow-up responses of patients aged between 6 and 14 years who will present with crown fractures in their maxillary or mandibular permanent incisors.

Written informed consent will be obtained from the parents of all participating patients. The research will be carried out using a prospective observational design.

Initially, sociodemographic information as well as personal data such as the child's age and gender will be collected through a questionnaire designed for the parents. Additionally, trauma-related information-including the time, location, and cause of the injury-will be recorded in detail using a trauma assessment form developed for the study.

Each patient will undergo clinical and radiographic evaluations, and treatment planning and follow-up will be carried out based on these findings.

Conditions

  • Dental Trauma
  • Crown Fractures
  • Tooth Fractures

Interventions

PROCEDURE

Direct Composite Restoration

Application of direct composite resin to restore the fractured crown of permanent incisors.

PROCEDURE

Cvek Pulpotomy

Partial pulpotomy (Cvek technique) will be performed for complicated crown fractures with vital pulp exposure. The goal is to maintain pulp vitality using biodentin.

PROCEDURE

Endodontic Treatment

Root canal treatment will be applied to teeth with necrotic pulp or extensive pulp exposure not suitable for vital pulp therapy. Procedures will follow standard endodontic protocols.

PROCEDURE

Pulp Capping

In cases of minimal pulp exposure, a direct pulp capping procedure will be performed using biocompatible materials such as calcium hydroxide to preserve pulp vitality.

Sponsors & Collaborators

  • Inonu University

    lead OTHER

Principal Investigators

  • Tuba Aydan, Pediatric Dentistry Specialist · Inonu University Faculty of Dentistry

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
6 Years
Max Age
14 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-01
Primary Completion
2025-09-01
Completion
2025-09-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07131462 on ClinicalTrials.gov